Powder: -20°C for 3 years | In solvent: -80°C for 1 year
ATC 0175 hydrochloride 是一种具有口服活性的黑色素细胞浓缩激素1受体拮抗剂,具有强效性和选择性,ATC 0175 hydrochloride 对MCH1R、MCH2R、MCH1、5-HT2B 受体和5-HT1A 受体 具有亲和力 ,IC50分别为为13.5nM、<10,000 nM、13 nM、9.66 nM 和16.9 nM。ATC 0175 hydrochloride 在动物模型中表现出抗抑郁和抗焦虑作用。ATC0175可用于研究抑郁症和/或焦虑症。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 822 | 现货 | ||
5 mg | ¥ 1,830 | 现货 | ||
10 mg | ¥ 2,920 | 现货 | ||
25 mg | ¥ 5,950 | 现货 | ||
50 mg | ¥ 7,860 | 现货 | ||
100 mg | ¥ 10,800 | 现货 | ||
500 mg | ¥ 21,600 | 现货 |
产品描述 | ATC 0175 hydrochloride is an orally active melanocyte concentrating hormone 1 receptor antagonist that is potent and selective. ATC 0175 hydrochloride has affinity for MCH1R, MCH2R, MCH1, 5-HT2B receptors and 5-HT1A receptors with IC50s of 13.5 nM, >10,000 nM, 13 nM, 9.66 nM and 16.9 nM, respectively. ATC 0175 hydrochloride exhibits antidepressant and anxiolytic effects in animal models. aTC 0175 can be used to study depression and/or anxiety disorders. |
靶点活性 | MCH1:13 nM, 5-HT2B:9.66 nM, 5-HT1A:16.9 nM |
体外活性 | In vitro, assays showed that this compound is a potent antagonist with a high affinity for MCH1R. The receptor binding and the functional assay (MCH-induced increase in [Ca2+]) indicated that ATC0175 is a noncompetitive antagonist at MCH1Rs.[1] |
体内活性 |
ATC0175 (1, 3, 10 mg/kg ; p.o. ) treatment also exhibited antidepressant effects in the forced swimming test.[2]
ATC0175 displayed anxiolytic effects in numerous animal models of anxiety including the social interaction test, elevated plus-maze test, maternal separation-induced vocalization and stress-induced hyperthermia.[2] |
分子量 | 461.93 |
分子式 | C23H26ClF2N5O |
CAS No. | 510733-97-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Ethanol: 22.5 mg/mL (48.7 mM)
DMSO: 9.0 mg/mL (19.4 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
Ethanol / DMSO | 1 mM | 2.1648 mL | 10.8242 mL | 21.6483 mL | 54.1208 mL |
5 mM | 0.433 mL | 2.1648 mL | 4.3297 mL | 10.8242 mL | |
10 mM | 0.2165 mL | 1.0824 mL | 2.1648 mL | 5.4121 mL | |
Ethanol | 20 mM | 0.1082 mL | 0.5412 mL | 1.0824 mL | 2.706 mL |
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
ATC 0175 hydrochloride 510733-97-8 Endocrinology/Hormones GPCR/G Protein Neuroscience GPR 5-HT Receptor Melanin-concentrating Hormone Receptor (MCHR) ATC-0175 Hydrochloride ATC 0175 Hydrochloride ATC0175 Hydrochloride Inhibitor inhibitor inhibit